COPIOS PERICARDIUM MEMBRANE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2017-05-10 for COPIOS PERICARDIUM MEMBRANE manufactured by Tutogen Medical Gmbh.

Event Text Entries

[74828344] Rti/tmi will conduct a re-review of the product history record for copios pericardium membranes, packaging production records, environmental monitoring, distribution for related complaints associated to the lot. A follow-up med watch will be submitted. Implanted not available for return.
Patient Sequence No: 1, Text Type: N, H10


[74828345] It was reported that on (b)(6) 2016 a puros pi block and cancellous particulates and a copios pericardium membrane was implanted for a dental procedure with the follow up treatment he noticed dehiscence of suture in the grafted area, even though there was no infection. The block is still in its place but he wanted to report the delayed wound healing.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002924436-2017-00010
MDR Report Key6556853
Report SourceHEALTH PROFESSIONAL
Date Received2017-05-10
Date of Report2017-08-08
Date of Event2016-11-10
Date Mfgr Received2017-04-10
Date Added to Maude2017-05-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. CHARITY
Manufacturer Street11621 RESEARCH CIRCLE
Manufacturer CityALACHUA FL 32615
Manufacturer CountryUS
Manufacturer Postal32615
Manufacturer Phone3864188888
Manufacturer G1RTI SURGICAL INC
Manufacturer Street11621 RESEARCH CIRCLE
Manufacturer CityALACHUA FL 32615
Manufacturer CountryUS
Manufacturer Postal Code32615
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOPIOS PERICARDIUM MEMBRANE
Generic NamePERICARDIUM MEMBRANE , PRODUCT CODE NPL
Product CodeNPL
Date Received2017-05-10
Lot NumberNZ15160015
OperatorDENTIST
Device Availability*
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerTUTOGEN MEDICAL GMBH
Manufacturer AddressINDUSTRIESTR. 6 NEUNKIRCHEN, GERMANY 91077GM GM 91077 GM


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-05-10

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